Evidence map›Paper›PMID 32266845›Full record

ArticleThe Journal of international medical research2020

Rare missense variant p.Ala505Ser in the ZAK protein observed in a patient with split-hand/foot malformation from a non-consanguineous pedigree.

Christopher Ronald Funk, Elizabeth S Huey, Melanie M May, Yunhui Peng, Ekaterina Michonova, Robert G Best, Charles E Schwartz, Anna V Blenda

Open access · goldAbstract read
In one paragraph

Article in The Journal of international medical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 57% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Christopher Ronald FunkJ.C. Self Research Institute, Greenwood Genetic Center, Greenwood, SC, United States.ORCID https://orcid.org/0000-0002-4113-5038
Elizabeth S HueyDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC, United States.
Melanie M MayJ.C. Self Research Institute, Greenwood Genetic Center, Greenwood, SC, United States.
Yunhui PengComputational Biophysics and Bioinformatics Laboratory, Department of Physics and Astronomy, Clemson University, Clemson, SC, United States.
Ekaterina MichonovaDepartment of Chemistry and Physics, Erskine College, Due West, SC, United States.
Robert G BestDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC, United States.
Charles E SchwartzJ.C. Self Research Institute, Greenwood Genetic Center, Greenwood, SC, United States.
Anna V BlendaDepartment of Biomedical Sciences, University of South Carolina School of Medicine Greenville, Greenville, SC, United States.
University of South Carolina · USGreenwood Genetic Center · USClemson University · USEmory University · USErskine College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AllelesAmino Acid SubstitutionGenetic Predisposition to DiseaseMutation, MissenseAnimalsChromosome DeletionChromosomes, Human, Pair 7Disease Models, AnimalDNA Mutational AnalysisEvolution, MolecularGenetic Association StudiesHumansLimb Deformities, CongenitalMAP Kinase Kinase KinasesMiceMice, KnockoutMAP3K20 protein, humanMAP Kinase Kinase Kinasesapical ectodermal ridge (AER)chromosome region 7q21.3-q22.1 (chr. 7q21)distal-less homeobox-5 (DLX5)distal-less homeobox-6 (DLX6)leucine zipper containing kinase AZK (ZAK)Split-hand/foot malformation (SHFM)

Identifiers

PMID32266845
PMCPMC7144677
OpenAlexW3015012505

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.